Synthesis of cyclic organic compounds and metallocenes

ABSTRACT

A method comprising synthesizing a cyclic organic compound via reaction of an unsubstituted or substituted cyclopentene with an unsubstituted or substituted acrylic acid in the presence of phosphoric and/or sulfonic acid reagent to make the cyclic organic compound. Also, a method of synthesizing a ligand for a transition metal, and a related substituted ligand-metal complex and catalyst, from the unsubstituted or substituted cyclopentene and unsubstituted or substituted acrylic acid. Also, the cyclic organic compound, ligand, and substituted ligand-metal complex and catalyst synthesized thereby. Also a method of polymerizing an olefin with the catalyst to give a polyolefin, and the polyolefin made thereby.

FIELD

Synthesizing cyclic organic compounds, and substituted metallocenestherefrom.

INTRODUCTION

Metallocene complexes comprise a transition metal atom that is bonded totwo ligands independently selected from an unsubstitutedcyclopentadienyl (Cp) ligand (formally an anion of formula C₅H₅) and/ora substituted cyclopentadienyl ligand, which is isolobal to Cp. Thetransition metal is an element of any one of Groups 3 to 12 useful forcatalyzing polymerizations of olefins. Examples of the transition metalare Group 4 metals such as titanium, zirconium, and hafnium. Examples ofthe substituted cyclopentadienyl ligands are methylcyclopentadienyl and4,5,6,7-tetrahydroindenyl. A typical metallocene complex is a4,5,6,7-tetrahydroindenyl-cyclopentadienyl zirconium dimethyl complex((4,5,6,7-tetrahydroindenyl)(cyclopentadienyl)Zr(CH₃)₂). Typically, thesynthesis of the complex involves numerous synthetic steps, usesexpensive reagents, and/or employs a platinum-catalyzed hydrogenationstep to convert an indenyl-cyclopentadienyl zirconium dichloridecompound to a 4,5,6,7-tetrahydroindenyl-cyclopentadienyl zirconiumdichloride compound. See, e.g., US 2004/0249096 A1 and U.S. Pat. No.5,721,185.

Uemichi, Yoshio; Kanoh, Hisao. Kenkyu Hokoku-Asahi Garasu Kogyo GijutsuShoreikai, Volume 49, Pages 225-30, 1986. CODEN:AGKGAA. ISSN:0365-2599report that platinum is especially potent source of polyethylenedegradation. Uemichi, Yoshio; Makino, Yutaka; Kanazuka, Takaji,Degradation of polyethylene to aromatic hydrocarbons overmetal-supported activated carbon catalysts, Journal of Analytical andApplied Pyrolysis (1989), 14(4), 331-44.

See also the following. Tabatabaenian, K.; Mamaghani, M.; Neshat, A.;Masjedi, M. Synthesis and Spectroscopic Studies of New SubstitutedDinuclear η⁵-4,5,6,7-Tetrahydroindenyl Ruthenium Complexes. RussianJournal of Coordination Chemistry. 2003, 29, 7, 501. Austin, R. N.;Clark, T. J.; Dickson, T. E.; Killian, C. M.; Nile, T. A.; Shabacker, D.J.; McPhail, T. A. Synthesis and Properties of Novel Substituted4,5,6,7-tetrahydroindenes and Selected Metal Complexes. Journal ofOrganometallic Chemistry. 1995, 491, 11. Conia, J. M.; Leriverend, M. L.Tetrahedron Letters. 1968, 17. 2101 (Conia et al.). L. Rand and R. J.Dolinski, J. Org. Chem., 1966, 31, 3063 and L. Rand and R. J. Dolinski,J. Org. Chem., 1966, 31, 4061 (collectively “Rand and Dolinski”).Yokota, K.; Kohsaka, T.; Ito, K.; Ishihara, N. Consideration ofMechanism of Styrene/Ethylene Copolymerization with Half-TitanoceneCatalysts. Journal of Polymer Science. 2005, 43, 5041. JP10316694A toTetsuya, I., et. al. Brancaccio G.; Lettieri, G.; Monforte, P.; Larizza,A. Farmaco, Edizione Scientifica. 1983, 9, 702-8. Eaton, P. E.; Carlson,G. R.; Lee, J. T. Phosphorus Pentoxide-Methanesulfonic Acid. AConvenient Alternative to Polyphosphoric Acid. J. Org. Chem. 1978, 38,4071. Paquette, L. A.; Stevens, K. E., Can. J. Chem. 1984, 62, 2415.Paquette, L. A.; Cheney, D. L., J. Org. Chem. 1989, 54, 3334. J. Org.Chem. 1966, 3065.

Conia, et al. reported that reacting cyclohexene and crotonic acid inpresence of polyphosphoric acid (PPA) exclusively gave as a sole product2,3,4,5,6,7-hexahydro-3-methyl-1H-inden-1-one (structure 1 in Conia etal.). Conia et al. reported reacting cyclopentyl crotonate or cyclohexylcrotonate in the presence of PPA gave3-methyl-bicyclo[3.3.0]-2-octen-1-one (40% yield, Table 1 in Conia etal.) or 2,3,4,5,6,7-hexahydro-3-methyl-1H-inden-1-one (60% yield, Table2 in Conia et al.), respectively.

Rand and Dolinski use polyphosphoric acid (PPA) or a mixture ofphosphorous pentoxide (P₂O₅ or P₄O₁₀) and PPA to catalyze the reactionof a cycloheptene, cyclohexene, or cyclopentene with analpha,beta-unsaturated carboxylic acid such as acrylic acid or crotonicacid gives a reaction mixture that contains or is free of an esterby-product such as cycloheptyl crotonate, cyclohexyl crotonate, orcyclopentyl crotonate. Relatively how much of the ester by-product ismade is said to depend on the amount of phosphorous pentoxide used inthe mixture with PPA or the amount of the PPA or P₂O₅/PPA mixturerelative to the amount of cycloalkene.

SUMMARY

We discovered an alternative shorter synthesis of an (unsubstituted orsubstituted)-tetrahydropentalenyl-metal dichloride complex that does notuse a hydrogenation catalyst, a hydrogenation step, or a hydrogenationcatalyst filtration step. The inventive (unsubstituted orsubstituted)-tetrahydropentalenyl-metal dichloride complex made thereby,and the inventive (unsubstituted orsubstituted)-tetrahydropentalenyl-metal dimethyl catalyst madetherefrom, and polyolefins made therewith are beneficially free of(added) hydrogenation catalyst metals such as platinum, palladium,nickel, rhodium, and ruthenium. As discussed above, polyolefindegradation problems have been attributed to hydrogenation catalystmetals are reported in the literature, and thus the inventive polyolefinbeneficially would inherently avoid any such problem(s). As such, theinventive polyolefin could have longer stability or less degradationthan prior polyolefins made with a catalyst synthesized using ahydrogenation step. The instability or degradation could appear over along period of time as discoloration and/or a change in molecular weightdistribution of the polyolefin, or some other manifestation thereof.

The inventive method is applied to tetrahydropentalenyl systems andcomprises synthesizing a cyclic organic compound via reaction of anunsubstituted or substituted cyclopentene with an unsubstituted orsubstituted acrylic acid in the presence of phosphoric and/or sulfonicacid reagent to make the cyclic organic compound. Also, a method ofsynthesizing a ligand for a transition metal, and a related substitutedligand-metal complex and catalyst, from the unsubstituted or substitutedcyclopentene and unsubstituted or substituted acrylic acid. Also, thecyclic organic compound, ligand, and substituted ligand-metal complexand catalyst synthesized thereby. Also a method of polymerizing anolefin with the catalyst to give a polyolefin, and the polyolefin madethereby.

DETAILED DESCRIPTION

The Summary and Abstract are incorporated here by reference.

Certain inventive embodiments are described below as numbered aspectsfor easy cross-referencing. Additional embodiments are describedelsewhere herein.

Aspect 1. A method of synthesizing a bicyclo[3.3.0]octene compound, themethod comprising (A) contacting a compound of formula (1) (“compound(1)”):

wherein R1, R2, and R3 are independently H or (C₁-C₄)alkyl, or R1 and R3are bonded together to form a (C₁-C₄)alkylene and R2 is H or(C₁-C₄)alkyl, with a compound of formula (2) (“compound (2)”):

wherein R4 is H or (C₁-C₄)alkyl, in the presence of an effective amountof a phosphoric and/or sulfonic acid reagent and under reactionconditions sufficient to make a compound of formula (3) (“compound(3)”):

and/or its oxo/R4 regioisomer; wherein R1 to R4 are as defined above.The “/” in “oxo/R4 regioisomer” indicates the groups that are indifferent positions in the oxo/R4 regioisomer relative to the compound(3). That is, the positions of the oxo (═O) and R4 substituents areswitched with each other relative to their positions in the compound(3). Thus, in the oxo/R4 regioisomer the oxo is bonded to the carbonatom bearing R4 in compound (3) and the R4 in the oxo/R4 regioisomer isbonded to the carbon atom bearing the oxo in compound (3). Functionalgroups that are in different positions in other regioisomers describedbelow may be designated using “group/group” (e.g., R5/R4) in a similarmanner. In some aspects when each of R1 to R3 is H and R4 is methyl, thephosphoric and/or sulfonic acid reagent and contacting step (A) are freeof a polyphosphoric acid (PPA). In some aspects, the phosphoric and/orsulfonic acid reagent and contacting step (A) are free of PPA.

Aspect 2. A method of synthesizing a ligand for a transition metal, themethod comprising: (A) synthesizing the compound (3):

and/or its oxo/R4 regioisomer, according to step (A) of aspect 1,wherein R1 to R4 are as defined above (in aspect 1); (B) contacting thecompound (3) and/or its oxo/R4 regioisomer with either ahydride-functional reducing agent or a (C₁-C₄)alkyl lithium, underreaction conditions sufficient to make a compound of formula (4)(“compound (4)”):

and/or its (HO,R5)/R4 regioisomer, respectively, wherein R1 to R4 are asdefined above and R5 is either H or (C₁-C₄)alkyl, respectively; and (C)contacting the compound (4) and/or its (HO,R5)/R4 regioisomer withdehydration reaction conditions to make a compound of formula (5)(“compound (5)”):

and/or its R5/R4 regioisomer, respectively; wherein R1 to R5 are asdefined above. The “/” identifies the groups that are in differentpositions in the respective regioisomers relative to compound (4) or(5). In some aspects the method further comprises a separation stepbetween steps (A) and (B), the separation step comprising separating thecompound (3) from its oxo/R4 regioisomer to give a purified compound (3)and/or a purified oxo/R4 regioisomer. Alternatively, in some aspects themethod further comprises a separation step between steps (B) and (C),the separation step comprising separating the compound (4) from its(HO,R5)/R4 regioisomer to give a purified compound (4) and/or a purified(HO,R5)/R4 regioisomer. Alternatively, in some aspects the methodfurther comprises a separation step after step (C), the separation stepcomprising separating the compound (5) from its R5/R4 regioisomer togive a purified compound (5) and/or a purified R5/R4 regioisomer. Methodsteps downstream from one of the separation steps may be free of eitherthe separated compound or its regioisomer, as the case may be andultimately make the compound (5) that is free of its R5/R4 regioisomeror make the R5/R4 regioisomer that is free of the compound (5). Theseparation steps may comprise fractional distillation, fractionalcrystallization, or chromatography such as gas chromatography or liquidchromatography. E.g., room pressure, medium pressure or high pressureliquid chromatography on a silica gel column using one or more organicsolvents as eluent.

Aspect 3. A method of synthesizing a zirconocene dichloride complex, themethod comprising synthesizing the compound (5) and/or its R5/R4regioisomer according to steps (A) to (C) of aspect 2; (D) contactingthe compound (5) and/or its R5/R4 regioisomer with an alkyl lithiumunder reaction conditions sufficient to make a compound of formula (6)(“compound (6)”):

and/or its R5/R4 regioisomer, wherein R1 to R5 are as defined in aspect2; and (E) contacting the compound (6) and/or its R5/R4 regioisomer witha compound of formula (7) (“compound (7)”):

wherein R6 to R8 independently are H or (C₁-C₄)alkyl and R9 and R10independently are H, (C₁-C₄)alkyl, or R9 and R10 are bonded together andare a (C₃-C₅)alkylene, under reaction conditions sufficient to make acompound of formula (8) (“compound (8)”):

and/or its R5/R4 regioisomer, wherein R1 to R10 are as defined above.Method steps downstream from one of the separation steps describedpreviously may be free of either the separated compound or itsregioisomer, as the case may be and ultimately make the compound (8)that is free of its R5/R4 regioisomer or make the R5/R4 regioisomer thatis free of the compound (8). The compound (7) may be made by contactinga R6 to R10-functional cyclopentadiene with an alkyl lithium underreaction conditions sufficient to make a R6 to R10-functionalcyclopentadienyl lithium, and contacting the R6 to R10-functionalcyclopentadienyl lithium with zirconium tetrachloride under reactionconditions sufficient to make the compound (7), wherein R6 to R10 are asdefined above. The R6 to R10-functional cyclopentadiene may besynthesized by known methods or obtained from a commercial source. Insome aspects R6 to R10 are H. In some aspects R6 is methyl and R7 to R10are H. In some aspects R6 to R8 are H and R9 and R10 are bonded togetherand are a (C₃-C₅)alkylene. In some aspects the (C₃-C₅)alkylene is a1,3-propane-diyl; alternatively a 1,4-butanediyl; alternatively a1,5-pentanediyl. The compounds (7) and (8) wherein R9 and R10 are bondedtogether and are a (C₃-C₅)alkylene may be made by the inventive methodstarting from cyclopentene for R9 and R10 together being1,3-propane-diyl; cyclohexene for R9 and R10 together being1,4-butanediyl; or cycloheptene for R9 and R10 together being1,5-pentanediyl. Alternatively, the compounds (7) and (8) wherein R9 andR10 are bonded together and are a (C₃-C₅)alkylene may be made by aconventional synthetic route. In some aspects compound (8) is of formula(8a):

wherein R4 and R5 are independently as H or (C₁-C₄)alkyl.

Aspect 4. A method of synthesizing a zirconocene dimethyl complex, themethod comprising synthesizing the compound (8) and/or its R5/R4regioisomer according to steps (A) to (E) of aspect 3; and (F)contacting the compound (8) and/or its R5/R4 regioisomer with aneffective amount of methyl magnesium bromide under reaction conditionssufficient to make a compound of formula (9) (“compound (9)”):

and/or its R5/R4 regioisomer, wherein R1 to R10 are as defined above (inaspect 3). Method steps downstream from one of the separation stepsdescribed previously may be free of either the separated compound or itsregioisomer, as the case may be and ultimately make the compound (9)that is free of its R5/R4 regioisomer or make the R5/R4 regioisomer thatis free of the compound (9). In some aspects R6 to R10 are H. In someaspects R6 is methyl and R7 to R10 are H. In some aspects R6 to R8 are Hand R9 and R10 are bonded together and are a (C₃-C₅)alkylene. In someaspects the (C₃-C₅)alkylene is a 1,3-propane-diyl; alternatively a1,4-butanediyl; alternatively a 1,5-pentanediyl. The compound (9)wherein R9 and R10 are bonded together and are a (C₃-C₅)alkylene may bemade by the inventive method, alternatively by a conventional syntheticroute. In some aspects compound (9) is of formula (8a) as defined aboveexcept wherein each Cl is replaced by methyl.

Aspect 5. The method of any one of aspects 1 to 4, wherein thephosphoric and/or sulfonic acid reagent is a polyphosphoric acid (PPA);a mixture of a phosphorous pentoxide and methanesulfonic acid(“P₂O₅/H₃CSO₃H mixture”), or a reaction product thereof; or acombination of a PPA and a P₂O₅/H₃CSO₃H mixture, or a reaction productof thereof.

Aspect 6. The method of any one of aspects 1 to 5 wherein the phosphoricand/or sulfonic acid reagent is a polyphosphoric acid (PPA).

Aspect 7. The method of any one of aspects 1 to 5, wherein thephosphoric and/or sulfonic acid reagent is, or consists essentially of,the P₂O₅/H₃CSO₃H mixture, or a reaction product thereof. Alternativelythe phosphoric and/or sulfonic acid reagent may consist essentially ofan alkylsulfonic acid such as a (C₁-C₆)alkylsulfonic acid such asmethanesulfonic acid. The expression “consist essentially of” means thephosphoric and/or sulfonic acid reagent and step (A) are free of PPA. Insome aspects the P₂O₅/H₃CSO₃H mixture is a 0.1/1 (weight/weight)P₂O₅/H₃CSO₃H mixture, known as Eaton's reagent.

Aspect 8. The method of any one of aspects 1 to 5, wherein thephosphoric and/or sulfonic acid reagent is the combination of the PPAand the P₂O₅/H₃CSO₃H mixture, or a reaction product thereof. In someaspects the P₂O₅/H₃CSO₃H mixture is a 0.1/1 (weight/weight) P₂O₅/H₃CSO₃Hmixture, known as Eaton's reagent.

Aspect 9. The method of any one of aspects 1 to 8, characterized by anyone of limitations (i) to (ix): (i) wherein at least one of R1 to R3 isa (C₁-C₄)alkyl or R4 is H; (ii) wherein each of R1 to R4 is H; (iii)wherein each of R1 to R3 is H and R4 is methyl; (iv) wherein in compound(1) each of R2 and R3 is H and R1 is methyl; in compound (2) R4 ismethyl; and in compound (3) each of R2 and R3 is H and each of R1 and R4is methyl; and in its oxo/R4 regioisomer each of R1 and R3 is H and eachof R2 and R4 is each methyl; (v) wherein R1 and/or R2 is methyl and R3is H; (vi) wherein R1 is methyl, R2 is 1-methylethyl (i.e., isopropyl),and R3 is H; (vii) wherein R1 is 1-methylethyl (i.e., isopropyl), R2 ismethyl, and R3 is H; (viii) wherein R1 and R2 independently are(C₁-C₄)alkyl, R3 is H, and the stereochemistry of the carbon atom bondedto R1 is (R) and the stereochemistry to the carbon atom bonded to R2 is(S); and (ix) wherein R1 and R2 independently are (C₁-C₄)alkyl, R3 is H,and the stereochemistry of the carbon atom bonded to R1 is (S) and thestereochemistry to the carbon atom bonded to R2 is (R). Alternativelyany one of limitations (x) to (xxiii): (x) both (vi) and (viii); (xi)both (vi) and (ix); (xii) both (vii) and (viii); (xiii) both (vii) and(ix); (xiv) wherein R5 is H; (xv) wherein R5 is methyl; (xvi) both (i)and (xiv) or (xv); (xvii) both (ii) and (xiv) or (xv); (xviii) both(iii) and (xiv) or (xv); (xix) both (iv) and (xiv) or (xv); (xx) both(v) and (xiv) or (xv); (xxi) wherein R9 and R10 are bonded together andare a (C₃-C₅)alkylene; (xxii) both (xxi) and any one of (i) to (xx); and(xxiii) R1 and R3 are bonded together to form a (C₁-C₄)alkylene and R2is H or (C₁-C₄)alkyl.

Aspect 10. The compound (3) or its oxo/R4 regioisomer made by the methodof aspect 1, the compound (4) or its (HO,R5)/R4 regioisomer made by themethod of aspect 2, the compound (5) or its R5/R4 regioisomer made bythe method of aspect 2, the compound (6) or (8), or their respectiveR5/R4 regioisomer made by the method of aspect 3, or the compound (9) orits R5/R4 regioisomer made by the method of aspect 4; wherein thecompound or its regioisomer is free of platinum, palladium, nickel,rhodium, and ruthenium. The term “free of” means contains no detectablepresence of. In some aspects the compound is any one of compounds (8-1),(8-2), (8-3), (8-4), (8a), and (8a-1); alternatively compound (9-1);described later in the Examples.

Aspect 11. A method of polymerizing an olefin, the method comprisingcontacting ethylene and/or an alpha-olefin with a catalyst made bycontacting the compound (8) or (9), or its R5/R4 regioisomer, made bythe method of aspect 4, with an activator, under conditions sufficientto make a polyolefin polymer comprising a polyethylene homopolymer, anethylene/alpha-olefin copolymer, or a poly(alpha-olefin) homopolymer. Insome aspects the catalyst is made from compound (8); alternatively fromany one of compounds (8-1), (8-2), (8-3), (8-4), (8a), and (8a-1)described later in the Examples; alternatively from compound (9);alternatively from compound (9-1); described later in the Examples.

Aspect 12. The polyolefin polymer made by the method of aspect 11 andbeing free of platinum, palladium, nickel, rhodium, and ruthenium. Insome aspects the polyolefin polymer is characterized by a butyl branchfrequency (BBF) of 0.5 to less than 1.5, alternatively 0.6 to less than1.2, alternatively 0.6 to less than 1.0, measured according to the ButylBranch Frequency (BBF) Test Method, described later.

In another embodiment of any one of the foregoing aspects, exceptwherein 3,3-dimethyl-1-cyclopentene is used in place of the compound(1). The 3,3-dimethyl-1-cyclopentene is a geminal-dimethyl analog ofcyclopentene and is a derivative of compound (1) wherein R2 and R3 areH, R1 is methyl, and the carbon atom bearing R1 is substituted with asecond methyl. The embodiments yield analogs of compounds (3) to (6),(8) and (9) wherein R2 and R3 are H, R1 is methyl, and the carbon atombearing R1 is substituted with a second methyl.

Compound: a molecule or a collection of same molecules.

Contacting: physically touching. In synthesizing context, contacting maybe facilitated by a solvent that dissolves the compounds or materialsbeing contacted.

Copolymer: macromolecular compound containing, in the same molecularentity or molecule, constitutional units derived from polymerizing amonomer and units derived from polymerizing at least one differentmonomer (comonomer).

Free of a polyphosphoric acid: no added polyphosphoric acid (PPA),alternatively no added, or in situ generated, PPA.

Homopolymer: macromolecular compound containing, in the same molecularentity or molecule, constitutional units, each of which is derived frompolymerizing the same monomer.

Independently: without regard to or dependence on another.

Mixture: intimate blend of two or more compounds or materials.

Oxo: ═O. E.g., as bonded to carbon atom in a carbonyl group (C═O).

Reaction product: different molecular entity than that from which it ismade via a chemical reaction. The difference may be oxidation stateand/or covalent bond(s).

Reagent, in the context of a reaction (e.g., step (A)): compound ormixture added to a reaction system to cause or enhance a desiredchemical reaction.

Regioisomer: a positional isomer without any differences in bondmultiplicities.

“R_(#)” and “R_(#)”, wherein # means number, mean the same. E.g., R₁ andR1 are the same and mean a first R group; R₂ and R2 are the same andmean a second R group; and so on.

Step, in the context of the method of synthesizing: distinct chemicalreaction, often with distinct reaction conditions and/or physicalmanipulations.

Stereochemistry: isomerism due to differences in spatial arrangement ofatoms without any differences in connectivity or bond multiplicitiesbetween isomers.

Synthesizing: purposeful execution of one or more distinct chemicalreactions or steps to manufacture a reaction product.

Zirconocene: complex comprising a zirconium atom bonded to one or twounsubstituted or substituted cyclopentadienyl-type groups, andoptionally other ligands (e.g., CH₃, Cl).

Activator (for activating compound (9) and/or its R5/R4 regioisomer toform a catalyst). Also known as co-catalyst. Any metal containingcompound, material or combination of compounds and/or substances,whether unsupported or supported on a support material, that canactivate compound (9) and/or its R5/R4 regioisomer to give a catalystand an activator species. The activating may comprise, for example,abstracting at least one leaving group (e.g., at least one methyl) fromthe Zr of compound (9) or its R5/R4 regioisomer to give the catalyst.The activator may be a Lewis acid, a non-coordinating ionic activator,or an ionizing activator, or a Lewis base, an alkylaluminum, or analkylaluminoxane. The alkylaluminum may be a trialkylaluminum,alkylaluminum halide, or alkylaluminum alkoxide (diethylaluminumethoxide). The trialkylaluminum may be trimethylaluminum,triethylaluminum (“TEAI”), tripropylaluminum, triisobutylaluminum, andthe like. The alkylaluminum halide may be diethylaluminum chloride. Thealkylaluminoxane may be a methyl aluminoxane (MAO), ethyl aluminoxane,or isobutylaluminoxane. The activator may be a MAO that is a modifiedmethylaluminoxane (MMAO). The corresponding activator species may be aderivative of the Lewis acid, non-coordinating ionic activator, ionizingactivator, Lewis base, alkylaluminum, or alkylaluminoxane, respectively.The activator species may have a different structure or composition thanthe activator from which it is derived and may be a by-product of theactivation reaction. The metal of the activator typically is differentthan zirconium. The molar ratio of metal content of the activator tozirconium content of compound (9) and/or its R5/R4 regioisomer may befrom 1000:1 to 0.5:1, alternatively 300:1 to 1:1, alternatively 150:1 to1:1.

Alkyl means an unsubstituted univalent saturated acyclic hydrocarbonthat is straight chain (1 or more carbon atoms), branched chain (if 3 ormore carbon atoms), or cyclic (if 3 or more carbon atoms). Each(C₁-C₄)alkyl is independently methyl, ethyl, propyl, 1-methylethyl,butyl, 1-methylpropyl, 2-methylpropyl, or 1,1-dimethylethyl.Alternatively each (C₁-C₄)alkyl is independently a (C₁-C₃)alkyl;alternatively a (C₂-C₄)alkyl; alternatively (C₁-C₂)alkyl; alternatively(C₂-C₃)alkyl; alternatively (C₃-C₄)alkyl; alternatively methyl or(C₃)alkyl. In some aspects each (C₁-C₄)alkyl is independently a(C₁-C₃)alkyl and each (C₁-C₃)alkyl is independently methyl, ethyl,propyl, or 1-methylethyl; alternatively methyl, propyl, or1-methylethyl; alternatively methyl; alternatively ethyl; alternativelypropyl; alternatively 1-methylethyl. Substituted alkyl is an alkyl asdefined above except wherein one or more hydrogen atoms is formallyreplaced by a substituent such as unsubstituted alkyl, halogen, oralkylcarboxylic ester.

Alkyl lithium is a compound of formula alkyl-Li. Examples of alkyllithium are methyl lithium, ethyl lithium, propyl lithium, n-butyllithium, sec-butyl lithium, t-butyl lithium, and pentyl lithium. The(C₁-C₄)alkyl lithium is an alkyl lithium wherein the alkyl is methyl,ethyl, propyl, 1-methyl ethyl, butyl, 1-methylpropyl, 2-methylpropyl(sec-butyl), or 1,1-dimethylethyl (t-butyl).

Alkylene is unsubstituted divalent saturated acyclic hydrocarbon that isstraight chain (1 or more carbon atoms), branched chain (if 3 or morecarbon atoms), or cyclic (if 3 or more carbon atoms). Each(C₁-C₄)alkylene is independently methylene (CH₂), ethylene (CH₂CH₂),propylene (CH₂CH₂CH₂), 1-methylethylene (CH(CH₃)CH₂), butylene ((CH₂)₄),1-methylpropylene (CH(CH₃)CH₂CH₂), 2-methylpropylene (CH₂CH(CH₃)CH₂), or1,1-dimethylethylene (C(CH₃)₂CH₂. Substituted alkylene is an alkylene asdefined above except wherein one or more hydrogen atoms is formallyreplaced by a substituent such as unsubstituted alkyl, halogen, oralkylcarboxylic ester.

Bicyclo[3.3.0]octene compounds are molecules having a five-memberedcarbocyclic ring fused to a five-membered carbocyclic ring. One of thefive-membered carbocyclic ring may contain a carbon-carbon double bond,which may be shared at the fusion point with the other five-memberedcarbocyclic ring. Examples are (3), its oxo/R4 regioisomer, (4), its(HO,R5)/R4 regioisomer, (5), its R5/R4 regioisomer, (6), its R5/R4regioisomer, (8), its R5/R4 regioisomer, (9), and its R5/R4 regioisomer.

Combination of polyphosphoric acid (PPA) and a mixture of a phosphorouspentoxide and methanesulfonic acid (“P₂O₅/H₃CSO₃H mixture”) is aphysical blend of PPA and a preformed P₂O₅/H₃CSO₃H mixture or a physicalblend of PPA, P₂O₅, and H₃CSO₃H. In some aspects the method furthercomprises limitation (i) or (ii): (i) a step of preforming thecombination of PPA and P₂O₅/H₃CSO₃H mixture before the contacting step(A) and in the absence of at least one, alternatively each of thecompounds (1) to (3) and the oxo/R4 regioisomer; or (ii) wherein thecontacting step (A) further comprises contacting PPA and theP₂O₅/H₃CSO₃H mixture together in the presence of at least one,alternatively each of the compounds (1) and (2) to form the combinationof PPA and P₂O₅/H₃CSO₃H mixture in situ.

Compound means a molecule or collection of molecules. When R1 to R3 isH, compound (1) is cyclopentene. When at least one of R1 to R3 is(C₁-C₄)alkyl, compound (1) is a substituted cyclopentene. When R4 is H,the compound (2) has CAS number 79-10-7 and is known as acrylic acid.When R4 is methyl, the compound (2) has CAS number 107-93-7 and is knownas (E)-2-butenoic acid, crotonic acid, or (trans) 3-methylacrylic acid.Compounds (1) and (2) are widely available from commercial suppliers.

Dehydration reaction conditions include temperature and reagentseffective for enhancing rate of loss of water from compound (4) and/orits (HO,R5)/R4 regioisomer. Example of such reagents are 1 Molar (M) orhigher hydrochloric acid (aqueous HCl) or anhydrous HCl or Amberlyst 15solid acid catalyst in an organic solvent such as ethanol,tetrahydrofuran or toluene. The hydrochloric acid may be from 1 M to 8M, alternatively from 2 M to 6 M.

Effective amount is a quantity sufficient for enabling the making of adetectable amount of intended product. An effective amount of thephosphoric and/or sulfonic acid reagent is a quantity thereof sufficientfor enabling the making of a detectable amount of compound (3) and/orits oxo/R4 regioisomer. Detectable amounts may be detected, andoptionally characterized, by any suitable analytical method such as1H-nuclear magnetic resonance (1H-NMR), high performance liquidchromatography (HPLC, versus a known standard), gas chromatography (GC,versus a known standard), or mass spectrometry; typically 1H-NMR. Theeffective amount of the phosphoric and/or sulfonic acid reagent used instep (A) may vary depending upon its composition, reaction conditions,and costs. A skilled person may determine an optimal effective amountthereof by starting with an initial reaction mixture of (1), (2), and 95wt % of the phosphoric and/or sulfonic acid reagent, and thereaftersystematically try reaction mixtures containing lower wt % of thephosphoric and/or sulfonic acid reagent until an optimal result underthe reaction conditions is found. When the phosphoric and/or sulfonicacid reagent is PPA, the P₂O₅/H₃CSO₃H mixture, or the combination of PPAand P₂O₅/H₃CSO₃H mixture, the effective amount may be from 50 to 95 wt%, alternatively from 50 to 80 wt % based on total weight of (1), (2),and the phosphoric and/or sulfonic acid reagent. Alternatively, theeffective amount of the P₂O₅/H₃CSO₃H mixture may be from 1 to 10 moleequivalents, alternatively 1 to 5 mole equivalents, alternatively 1 to 3mole equivalents thereof relative to the number of moles of compound(1). For example, if 1.0 mole of compound (1) is used in the contactingstep (A), then the effective amount of the P₂O₅/H₃CSO₃H mixture may befrom 1 to 10 moles, alternatively from 1 to 5 moles, alternatively from1 to 3 moles.

Hydride-functional reducing agent means a compound having a metal-H bondcapable of adding to an oxo group of a ketone to give a tertiaryalcohol. Suitable metals include Al and B. Suitable hydride-functionalreducing agents are lithium aluminum hydride (LiAlH₄), diisobutylaluminum hydride (i-Bu₂AlH), and sodium borohydride (NaBH₄).

Methanesulfonic acid is a compound of formula H₃CSO₃H and has CAS number75-75-2 and is widely available from commercial suppliers.

Mixture of a phosphorous pentoxide and methanesulfonic acid orP₂O₅/H₃CSO₃H mixture is a blend or reaction product of phosphorouspentoxide and methane sulfonic acid. The weight/weight ratio ofP₂O₅/H₃CSO₃H in the mixture may be from 0.1 to 1 alternatively 0.15 to1, alternatively 0.2 to 1. The 0.1/1 (wt/wt) P₂O₅/H₃CSO₃H mixture iscommercially available and may be referred to as Eaton's reagent. Themixture of P₂O₅ and CH₃SO₃H may be formed in situ in the presence of thecompound (1) and/or (2), such as prior to or during the contacting step(A). Alternatively, the mixture of P₂O₅ and CH₃SO₃H may be preformedbefore contacting step (A). It is convenient to preform the P₂O₅/CH₃SO₃Hmixture before contacting step (A), and store the resulting preformedmixture for later use in embodiments of the contacting step (A). In someaspects the method further comprises limitation (i) or (ii): (i) a stepof preforming the P₂O₅/H₃CSO₃H mixture before the contacting step (A)and in the absence of at least one, alternatively each of the compounds(1) and (2); or (ii) wherein the contacting step further comprisescontacting a phosphorous pentoxide and methanesulfonic acid together inthe presence of at least one, alternatively each of the compounds (1)and (2) to form the P₂O₅/H₃CSO₃H mixture in situ.

Phosphoric and/or sulfonic acid reagent is an acidic material havingO—P(O)—OH acid groups and/or C—S(O)₂—OH acid groups, or an acidicreaction product thereof. The phosphoric and/or sulfonic acid reagentmay be, or may consist essentially of, a mixture of a phosphorouspentoxide and methanesulfonic acid (“P₂O₅/H₃CSO₃H mixture”), or areaction product thereof; alternatively a polyphosphoric acid (PPA);alternatively a combination of a P₂O₅/H₃CSO₃H mixture and a PPA, or areaction product thereof. In some embodiments the phosphoric and/orsulfonic acid reagent consists essentially of the P₂O₅/H₃CSO₃H mixture.Alternatively the phosphoric and/or sulfonic acid reagent may consistessentially of an alkylsulfonic acid such as a (C₁-C₆)alkylsulfonic acidsuch as methanesulfonic acid. The expression “consist essentially of”means the phosphoric and/or sulfonic acid reagent and step (A) are freeof PPA.

Polyphosphoric acid or PPA has CAS no. 8017-16-1 and is a compoundgenerally of formula HO—[P(═O)(OH)]_(n)—H, wherein subscript n indicatesdegree of polymerization. PPAs are widely available from commercialsuppliers.

Phosphorous pentoxide is a compound of formula P₂O₅ and has CAS number1314-56-3 and is widely available from commercial suppliers.

In some aspects each reactant, reagent, solvent, or other material usedin the inventive methods, and each product thereof, is free of Pt, Ni,Pd, Rh, and Ru.

The “reaction conditions sufficient to make” mean appropriate for thedesired chemical transformation, as is well understood in the art, andinclude reaction temperature; reaction pressure; reaction atmosphere;reaction solvent, if any; reactant and reagent concentrations; molarratios of reactants to each other and to reagents; and absence ofnegating compounds. Reaction pressure is typically room pressure (e.g.,101 kilopascals (kPa), except higher for olefin polymerizationreactions. If desired reactions (e.g., steps (A) to (F)) may be carriedout in a fume hood under an anhydrous molecular nitrogen gas atmosphereor using Schlenck line techniques and conditions.

Reaction temperatures under reaction conditions sufficient to make mayvary from step to step. For example, in step (A) (cyclocondensation)when the phosphoric and/or sulfonic acid reagent is PPA, the underreaction conditions sufficient to make compound (3) and/or its oxo/R4regioisomer may include a reaction temperature of at least 40° C.,alternatively at least 50° C., alternatively at least 65° C.; and atmost 100° C., alternatively at most 95° C., alternatively at most 90°C., alternatively at most 80° C. In step (A) when using the P₂O₅/H₃CSO₃Hmixture the reaction temperature may be from −78° to 30° C.,alternatively from −30° to 25° C., alternatively from 0° to 25° C. Insteps (B) (hydride reduction or alkyl lithium addition), (D)(deprotonation of a cyclopentadiene), (E) (forming a zirconocenedichloride) and (F) (forming a zirconocene dimethyl) the reactiontemperatures may be independently from −30° to 110° C., alternativelyfrom 0° to 50° C., alternatively from 10° to 30° C. In step (C)(dehydration) the reaction temperature may be from 0° to 120° C.,alternatively from 20° to 110° C., alternatively from 30° to 100° C.

The use or not of solvent and the type of solvent if used under reactionconditions sufficient to make may vary from step to step. Step (A) maybe free of solvent or may employ a solvent. When the phosphoric and/orsulfonic acid reagent is PPA, a solvent may be omitted. When thephosphoric and/or sulfonic acid reagent is the P₂O₅/H₃CSO₃H mixture, apolar aprotic solvent may be employed. The polar aprotic solvent may beselected from sulfolane, 1,2-dimethoxyethane,1-methoxy-2-(2-methoxyethoxy)ethane, and mixtures of any two or morethereof. The amount of polar aprotic solvent employed is notparticularly important. The foregoing polar aprotic solvents may serveto solubilize the compounds (1) and (2) and/or the P₂O₅/H₃CSO₃H mixture.The amount of solvent employed may be sufficient to prepare a startingsolution of that is from 0.5 Molar (M) to 5 M, or 1 M to 2.5 M ofP₂O₅/H₃CSO₃H mixture in the compound (2). The polar aprotic solvent mayallow the contacting step (A) to be performed at lower temperatureswithin the ranges given above therefor. A polar aprotic solvent is usedfor the P₂O₅/H₃CSO₃H mixture because a protic solvent is expected toundesirably react with the P₂O₅/H₃CSO₃H mixture, which is a powerfuldehydrating agent. The polar aprotic solvent may be of intermediatepolarity in order to co-solubilize the compounds (1) and (2) andP₂O₅/H₃CSO₃H mixture. The polar aprotic solvent may be capable ofproducing a homogeneous solution of the compounds (1) and (2) at 25° C.,alternatively at 10° C., alternatively at 0° C. A homogeneous solutionis not required for successful reaction of compounds (1) and (2) in thepresence of the phosphoric and/or sulfonic acid reagent. In steps (B)(hydride reduction or alkyl lithium addition), (D) (deprotonation of acyclopentadiene), (E) (forming a zirconocene dichloride) and (F)(forming a zirconocene dimethyl) an anhydrous, non-polar aprotic solventsuch as an alkyl ether such as diethyl ether, tetrahydrofuran, ordioxane may be used. In step (B) when the hydride-functional reducingagent is used and is lithium aluminum hydride or diisobutyl aluminumhydride, the anhydrous, non-polar solvent is used. In step (B) when thehydride-functional reducing agent is used and is sodium borohydride, apolar protic solvent may be used such as methanol, ethanol, 2-propanol,or 1-methoxy-2-(2-methoxyethoxy)ethane. The alkyl lithium reagent may bedissolved in anhydrous alkane solvent such as hexanes, hexane, orheptane. Grignard reagents such as methyl magnesium bromide may bedissolved in an alkyl ether such as dialkyl ether.

Reaction atmosphere included under reaction conditions sufficient tomake may be anhydrous molecular nitrogen gas or Schlenck line conditionsfor step (A) (cyclocondensation) and air for step (C) (dehydrating).Reaction atmosphere for step (B) (hydride reduction or alkyl lithiumaddition), (D) (deprotonation of a cyclopentadiene), (E) (forming azirconocene dichloride) and (F) (forming a zirconocene dimethyl) may bean inert gas such as anhydrous nitrogen, argon or helium gas, or amixture of any two or more thereof.

Reaction concentrations of reactants and reagents included underreaction conditions sufficient to make may be independently in the rangefrom 0.1 to 1.4 M, alternatively 0.25 to 1 Molar (M), alternatively 0.4to 1 M.

Molar ratios of reactants to each other and to reagents included underreaction conditions sufficient to make may vary from 0.25 times to 1.5times theoretical reaction stoichiometry, alternatively from 0.99 timesto 1.2 times theoretical reaction stoichiometry, alternatively from 1.0to 1.1 times theoretical reaction stoichiometry, depending upon thereactants and reagents used. In step (A) (cyclocondensation) thetheoretical reaction stoichiometry of compound (1) to compound (2) is1.0 to 1.0. In step (B) (hydride reduction or alkyl lithium addition),the theoretical reaction stoichiometry of the hydride-functionalreducing agent to compound (3) (or its regioisomer) is 0.25 LiAlH4 orNaBH4 to 1.0 compound (3) and 0.5 DIBAL-H to 1.0 compound (3) and 1.0(C₁-C₄)alkyl lithium to 1.0 compound (3) (or its regioisomer). Thetheoretical reaction stoichiometry for step (C) (dehydration) iscatalytic in acid catalyst up to, typically, 1:1. The theoreticalreaction stoichiometry for each of steps (D) (deprotonation of acyclopentadiene), or (E) (forming a zirconocene dichloride) is typically1:1. The theoretical reaction stoichiometry for step (F) (forming azirconocene dimethyl) is 2.0 methyl magnesium bromide to 1.0 compound(8) (or its R5/R4 regioisomer).

Negating agents should not be included under reaction conditionssufficient to make. In step (A) (cyclocondensation), a negating agentmay be a quantify of a basic compound that would neutralize the acidityof the phosphoric and/or sulfonic acid reagent or otherwise render itineffective; or a negating agent may be an unsaturated aliphaticcompound that would react with compound (2) before compound (2) couldreact with compound (1). In steps (B) (hydride reduction or alkyllithium addition), (D) (deprotonation of a cyclopentadiene), (E)(forming a zirconocene dichloride) and (F) (forming a zirconocenedimethyl), a negating agent would be a protic compound (e.g., a NHfunctional, OH functional, and/or SH functional compound) or a strongoxidizing agent. Examples of NH functional compounds are primary andsecondary amines and amides. Examples of OH functional compounds arealcohols, carboxylic acids, and oximes. Examples of SH functionalcompounds are thiols (mercaptans). Examples of NH and OH functionalcompounds are primary and secondary amino alcohols and amino acids. Instep (C) (dehydrating), a negating agent would be added water (notcounting water formed as a by-product of the dehydrating step) or aquantity of a basic compound that would neutralize an acid dehydrationcatalyst used therein.

A compound includes all its isotopes and natural abundance andisotopically-enriched forms. The enriched forms may have medical oranti-counterfeiting uses.

In some aspects any compound, composition, formulation, mixture, orreaction product herein may be free of any one of the chemical elementsselected from the group consisting of: H, Li, Be, B, C, N, O, F, Na, Mg,Al, Si, P, S, Cl, K, Ca, Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Ga, Ge,As, Se, Br, Rb, Sr, Y, Zr, Nb, Mo, Tc, Ru, Rh, Pd, Ag, Cd, In, Sn, Sb,Te, I, Cs, Ba, Hf, Ta, W, Re, Os, Ir, Pt, Au, Hg, Tl, Pb, Bi,lanthanoids, and actinoids; with the proviso that chemical elementsrequired by the compound, composition, formulation, mixture, or reactionproduct (e.g., C and H required by a polyolefin or C, H, and 0 requiredby an alcohol) are not excluded.

The following apply unless indicated otherwise. Alternatively precedes adistinct embodiment. ASTM means the standards organization, ASTMInternational, West Conshohocken, Pa., USA. Any comparative example isused for illustration purposes only and shall not be prior art. Free ofor lacks means a complete absence of; alternatively not detectable. Mayconfers a permitted choice, not an imperative. Operative meansfunctionally capable or effective. Optional(ly) means is absent (orexcluded), alternatively is present (or included). Properties aremeasured using a standard test method and conditions for the measuring(e.g., viscosity: 23° C. and 101.3 kPa). Ranges include endpoints,subranges, and whole and/or fractional values subsumed therein, except arange of integers does not include fractional values. Room temperature:23° C.±1° C. Substituted when referring to a compound means having, inplace of hydrogen, one or more substituents, up to and including persubstitution.

EXAMPLES

Unless noted otherwise herein, use the following preparations forcharacterizations. Carry out syntheses under an atmosphere of drynitrogen in a glovebox when indicated. Perform reactions requiringanhydrous conditions under an atmosphere of dry nitrogen in oven-driedglassware cooled under a stream of dry nitrogen. Anhydrous toluene,hexanes, tetrahydrofuran, diethyl ether and 1,2-dimethoxyethane are fromSigma-Aldrich. Solvents that are used for experiments performed in anitrogen-filled glovebox are further dried by storage over activated 4Angstrom (Å) molecular sieves. Cyclopentadienylzirconium (IV) chloride(compound (7) wherein R6-R10 is H, “(Cp)ZrCl₃”) and zirconium (IV)chloride (ZrCl₄) complex with dimethoxyether (DME) are purchased fromBoulder Scientific and is used as received.Methylcyclopentadienylzirconium (IV) chloride (compound (7) whereinR6-R9 is H and R10 is methyl, “(MeCp)ZrCl₃”) is purchased as a complexwith DME from Boulder Scientific and is used as received.Propylcyclopentadienylzirconium (IV) chloride (compound (7) whereinR6-R9 is H and R10 is propyl, “(PrCp)ZrCl₃”) is purchased as a complexwith DME from Boulder Scientific and is used as received.Tetramethylcyclopentadienylzirconium (IV) chloride (compound (7) whereinR6-R9 is methyl and R10 is H, “(Me₄Cp)ZrCl₃”) is purchased from BoulderScientific and is used as received. All other reagents are purchasedfrom Sigma-Aldrich and are used as received. For example, P₂O₅/CH₃SO₃H(0.1/1 wt/wt) may be purchased from Sigma-Aldrich, CAS #39394-84-8.

¹H-NMR (proton nuclear magnetic resonance spectroscopy) chemical shiftdata are reported in parts per million (ppm) down field relative totetramethylsilane (TMS), δ scale, using residual protons in deuteratedsolvent as references. The ¹H-NMR chemical shift data measured in CDCl₃are referenced to 7.26 ppm, data measured in benzene-d6 (C₆D₆) to 7.16ppm, data measured in tetrahydrofuran-d8 (THF-d8) to 3.58 ppm. ¹H-NMRchemical shift data are reported in the format: chemical shift in ppm(multiplicity, coupling constant(s) in Hertz (Hz), and integrationvalue. Multiplicities are abbreviated s (singlet), d (doublet), t(triplet), q (quartet), pent (pentet), m (multiplet), and br (broad).

GC/MS (EI) means gas chromatography-mass spectrometry (electronionization). Butyl Branch Frequency (BBF) Test Method: Butyl BranchingFrequency is number of butyl branches per 1000 main chain carbon atomsof a poly(ethylene-co-1-hexene) copolymer. To prepare test sample, addapproximately 2.74 g of a 50/50 mixture oftetrachloroethane-d₂/orthodichlorobenzene containing 0.025 M Cr(AcAc)₃to 0.15 g of test sample of the copolymer in a 10 mm NMR tube (Norell1001-7). Remove oxygen manually by purging tube with nitrogen using aPasteur pipette for 1 minute. Dissolve and homogenize test sample byheating the tube and its contents to 150° C. in a heating block.Visually inspect heated test sample to ensure homogeneity (thoroughmixing). Without allowing heated test sample to cool, insert it into aheated (120° C.) NMR probe. Allow inserted sample to thermallyequilibrate at the probe temperature for seven minutes. Then acquire NMRdata using a Bruker 400 MHz spectrometer, equipped with a BrukerCryoProbe using 320 transient scans, and a six second pulse repetitiondelay. Make all measurements on a non-spinning sample in locked mode.Internally reference ¹³C NMR chemical shifts to the EEE triad at 30 ppm.Determine short chain branches (SCB) derived from 1-hexene (C4 branches)comonomeric units by setting the integral value for the entire spectrum(from ˜40 to 10 ppm) to 1,000, and then calculate BBF according to thefollowing formula: BBF=(a+b/2+c+d/2+e)/5, wherein a, b, c, d, e and fare the integrated regions of the ¹³C NMR signals at 38.2, 34.6, 34.2,27.3 and 23.4 ppm, respectively.

Melt Temperature Test Method: melt temperature of a polymer isdetermined by Differential Scanning calorimetry according to ASTM D3418-08. For instance, using a scan rate of 10° C./minute on a sample of10 mg and using the second heating cycle.

Molecular Weights Test Method: determine molecular weights (MW)including weight-average molecular weight (Mw), number average molecularweight (Mn), and z-average molecular weight (Mz), and calculatemolecular weight distribution (Mw/Mn or MWD) by using a High TemperatureGel Permeation Chromatography (Polymer Laboratories), equipped with adifferential refractive index detector (DRI). Use three PolymerLaboratories PLgel 10 μm Mixed-B columns, nominal flow rate 1.0milliliter per minute (mL/min.), and nominal injection volume 300microliters (μL). House transfer lines, columns, and differentialrefractometer (the DRI detector) in an oven maintained at 160° C.Measure all quantities gravimetrically. Prepare solvent by dissolving 6grams of butylated hydroxytoluene (antioxidant) in 4 liters of reagentgrade 1,2,4-trichlorobenzene (TCB). Filter the TCB mixture through a 0.1micrometer (μm) Teflon filter. Degas the filtrate with an in-linedegasser before it enters the GPC instrument. Prepare test polymersolutions by placing test sample of dry polymer in glass vials, addingan amount of TCB sufficient to give an injection concentration from 0.5to 2.0 mg/mL, using lower concentrations for higher molecular weightsamples. Then heat the mixture at 160° C. with continuous shaking for 2hours to give a ready test sample. Prior to running each ready testsample, purge the DRI detector. Before injecting each ready test sample,increase flow rate in the apparatus to 1.0 mL/min., and allow the DRIdetector to stabilize for 8 hours. Determine molecular weights (MW) bycombining universal calibration relationship with the columncalibration, which is performed with a series of monodispersedpolystyrene (PS) standards. Calculate MW at each elution volume withfollowing equation:

${{\log M_{X}} = {\frac{\log\left( {K_{X}\text{/}K_{PS}} \right)}{a_{X} + 1} + {\frac{a_{PS} + 1}{a_{X} + 1}\log M_{PS}}}},$wherein subscript “X” indicates test sample and subscript “PS” indicatesPS standard. In this method, a_(PS)=0.67 and K_(PS)=0.000175 and obtaina_(X) and K_(X) from published literature. Specifically,a/K=0.695/0.000579 for polyethylenes (PE) and 0.705/0.0002288 forpolypropylenes (PP). Calculate concentration, c, at each point in thechromatogram from the baseline-subtracted DRI signal, I_(DRI), using thefollowing equation: c=K_(DRI)I_(DRI)/(dn/dc), where K_(DRI) is aconstant determined by calibrating the DRI, and (dn/dc) is therefractive index increment for the system. Specifically, dn/dc=0.109 forpolyethylene. Calculate mass recovery from the ratio of the integratedarea of the concentration chromatography over elution volume and theinjection mass, which is equal to the pre-determined concentrationmultiplied by injection loop volume. Report all molecular weights ing/mol unless otherwise noted. In event of conflict between the GPC-DRIprocedure and the “Rapid GPC,” the GPC-DRI procedure immediately aboveshall be used. If desired, see US 2006/0173123 A1, pages 24-25,paragraphs [0334] to [0341], for further details on determining Mw, Mn,Mz, MWD.

Inventive Example 1: synthesis of compound (3-1) (compound (3) whereinR1 to R3 is H and R4 is methyl) using P₂O₅/H₃CSO₃H mixture: In a fumehood, under a nitrogen atmosphere in a 250 mL round bottom flaskequipped with a stir bar, (E)-2-butenoic acid (compound (2) wherein R4is methyl, 5 g, 57.5 millimoles (mmol)) is added followed bycyclopentene (compound (1) wherein R1 to R3 is H, 5.6 mL, 63.3 mmol).The reaction mixture is cooled to 0° C. Next, P₂O₅/H₃CSO₃H mixture(0.1/1) is added dropwise (55.3 mL, 348 mmol) at 0° C. The reactionmixture, with stirring, is warmed up to room temperature and thenstirring is continued for 20 hours. The resulting crude product isdiluted with 50 mL of water. Solid NaHCO₃ is added until bubblingsubsides. The reaction mixture reaches pH 8 to pH 9. The aqueous andorganic layers are separated in a separatory funnel. The aqueous layeris extracted three times with diethyl ether (3×50 mL). The organiclayers are combined and washed with brine (50 mL), dried over anhydrousmagnesium sulfate and filtered. The solvent is removed in vacuo toafford 5.7 g of compound (3-1) as a dark brown liquid product (72%yield). Compound (3-1) was characterized by ¹H-NMR and GC/MS (EI).¹H-NMR (400 MHz, CDCl₃) δ 2.87 (ddt, 1H), 2.83-2.72 (m, 1H), 2.56-2.44(m, 1H), 2.41-2.17 (m, 6H), 1.10 (d, 3H).

Inventive Example 2: synthesis of compound (3-1) (compound (3) whereinR1 to R3 is H and R4 is methyl) using PPA:A 3-necked, 250 mL roundbottom flask fitted with a mechanical stirrer and under a nitrogenatmosphere is charged with polyphosphoric acid (PPA) (66 g) and warmedup to 65° C. until the PPA becomes soluble. (E)-2-butenoic acid(compound (2) wherein R4 is methyl, also known as crotonic acid, 3.0 g,34.8 mmol) is added, followed by the dropwise addition of cyclopentene(compound (1) wherein R1 to R3 is H, 3.08 mL, 34.8 mmol). The resultingreaction mixture turns bright orange. The reaction mixture ismechanically stirred at 65° C. for 1.5 hours. The resulting dark brownthick reaction mixture is poured onto ice/water. The mixture isextracted three times with diethyl ether (3×60 mL). The organic layersare combined with saturated aqueous sodium bicarbonate (100 mL), andstirred for 20 minutes until bubbling subsides. The organic layer isseparated and is further washed with saturated bicarbonate (2×60 mL).The organic layer is washed with brine (60 mL), dried over anhydrousmagnesium sulfate, and filtered. The solvent is removed in vacuo, theobtained product was refined by silica gel chromatography (diethylether/hexane) to afford 1.2 g of compound (3-1) as a light brown liquid(24% yield). ¹H-NMR (400 MHz, CDCl₃) δ 2.93 (dd, 1H), 2.88-2.78 (m, 1H),2.63-2.48 (m, 1H), 2.47-2.23 (m, 6H), 1.16 (d, 3H).

Inventive Example 3: synthesis of compound (4-1): compound (4) whereinR1 to R3 is H and R4 and R5 are methyl. Under an atmosphere of drynitrogen, the compound (3-1) of Inventive Example 2 (1.1 g, 8.08 mmol)is weighed out in a 100 mL round bottom flask and is dissolved inanhydrous diethyl ether (17 mL). The reaction mixture is cooled to −78°C. Methyl lithium (1.6 M, 6.31 mL, 10.1 mmol) is added dropwise and thesolution is stirred for 15 minutes at −78° C. The reaction mixture isstirred for 20 hours at room temperature to give a reaction mixturecontaining compound (4-1). Compound (4-1) was not isolated orcharacterized by ¹H-NMR. It may be characterized by GC/MS (EI).

Inventive Example 4: synthesis of compound (5-1): compound (5) whereinR1 to R3 is H and R4 and R5 are methyl. The reaction mixture containingcompound (4-1) in Inventive Example 3 is hydrolyzed by the addition ofaqueous 6 M HCL (5.3 mL) and stirring for 20 hours at room temperature.The organic phase is separated and the aqueous layer is extracted withdiethyl ether (2×25 mL). The combined organic layers are washed withwater (50 mL), followed saturated NaHCO₃ (50 mL) and brine (50 mL). Theorganic layers are dried over magnesium sulfate and filtered, and thesolvent is removed in vacuo. The obtained product was refined by passingit through a silica gel plug and eluting with diethyl ether/hexane togive 0.7 g of compound (5-1) in 65% overall yield from compound (3-1) ofInventive Example 2. Obtained as a mixture of double bond regioisomers.¹H-NMR (400 MHz, CDCl₃) δ 3.16-2.98 (m, 2H), 2.43-1.88 (series ofmultiplets, 13H).

Inventive Example 5: synthesis of compound (6-1): compound (6) whereinR1 to R3 is H and R4 and R5 are methyl. In a glove box, in a 120 mLglass jar, compound (5-1) (0.7 g, 5.22 mmol) is dissolved in hexanes (26mL). To the stirred solution is added dropwise a solution of n-butyllithium in hexanes (1.6 M, 3.92 mL, 6.27 mmol). The reaction mixture isstirred for 20 hours. The compound (6-1) is collected by vacuumfiltration, and the resulting solid product is washed with hexanes anddried under vacuum to give 0.28 g of compound (6-1) in 38% yield. ¹H-NMR(400 MHz, THF-d₈) δ 5.02 (s, 1H), 2.37 (m, 4H), 2.11 (m, 2H), 1.89 (s,6H).

Inventive Example 6: synthesis of compound (8-1): compound (8) whereinR1 to R3 and R6 to R10 are H and R4 and R5 are methyl. In drybox in a120 mL glass jar, (Cp)ZrCl₃ (compound (7) wherein R6 to R10 are H, 0.52g, 1.97 mmol) is slurried in 9 mL of 1,2-dimethoxyethane and stirred. Tothe stirred reaction mixture is added compound (6-1) (0.28, 1.97 mmol)in small portions. The resulting reaction mixture is stirred for 48hours at room temperature. The resulting reaction mixture was evaporatedin vacuo to remove the solvent. The resulting solid was extracted withdichloromethane and filtered to give 0.21 g of compound (8-1) in 30%yield. ¹H-NMR (400 MHz, Benzene-d₆) δ 6.01 (s, 5H), 5.34 (s, 1H), 2.94(m, J=2H), 2.34-2.16 (m, 3H), 2.05-1.87 (m, 1H), 1.66 (s, 6H).

Inventive Example 7 (prophetic): compound (9-1): compound (9) wherein R1to R3 and R6 to R10 are H and R4 and R5 are methyl. In drybox in an 240mL glass jar, compound (8-1) (10.5 mmol) is slurried in anhydrousdiethyl ether (65 mL). To the stirred reaction mixture is added asolution of methyl magnesium bromide (3.0 M, 7.89 mL, 23.7 mmol)dropwise. The reaction mixture is stirred for 20 hours at roomtemperature. The solvent is removed under vacuum. The resulting solidproduct is dissolved in hexanes (150 mL) and filtered. The hexanes areremoved under vacuum to afford compound (9-1).

Inventive Example 8 (prophetic): synthesis of compound (3-2) and itsoxo/R4 regioisomer using P₂O₅/H₃CSO₃H mixture: compound (3) wherein R1and R2 is H and R3 and R4 are methyl, and its oxo/R4 regioisomer. In afume hood under a nitrogen atmosphere, in a round bottom flask equippedwith a stir bar, (E)-2-butenoic acid (compound (2) wherein R4 is methyl,1 g, 11.6 mmol) is added followed by 4-methyl-1-cyclopentene (compound(1) wherein R3 is methyl, 11.6 mmol). Next, 1,2-dimethoxyethane is added(5.5 mL). The reaction mixture is cooled to −20° C. Next, addP₂O₅/H₃CSO₃H mixture (0.1:1) dropwise (5.53 mL, 34.8 mmol) at −20° C.The reaction mixture, with stirring, is warmed up to room temperatureand then stirring is continued for 20 hours. The mixture is diluted into50 mL of water and 50 mL of diethyl ether. Solid NaHCO₃ is added untilbubbling subsides. The liquid layer is decanted and the aqueous andorganic layers are separated. The aqueous layer is extracted twice withdiethyl ether (2×15 mL). The combined organic layers are combined andwashed with saturated NaHCO₃ (20 mL). The organic layer is washed withbrine (30 mL), dried over magnesium sulfate and filtered. The solvent isremoved in vacuo to afford compound (3-2) and its oxo/R4 regioisomer.

Inventive Example 9 (prophetic): polymerization of ethylene using acatalyst prepared from compound (8-1) or (9-1). Use a gas-phasefluidized bed reactor (“Reactor”) having a reaction zone dimensioned as304.8 mm (twelve inch) internal diameter and a 2.4384 meter (8 feet) instraight-side height and containing a fluidized reactor bed of polymergranules. Configure the Reactor with a recycle gas line for flowing arecycle gas stream. Fit the Reactor with gas feed inlets and polymerproduct outlet. Introduce gaseous feed streams of ethylene and hydrogentogether with liquid 1-hexene comonomer below the fluidized reactor bedinto the recycle gas line. Control individual flow rates of ethylene(“C2”), hydrogen (“H2”) and 1-hexene (“C6”) to maintain a fixed 1-hexenecomonomer to ethylene monomer composition molar ratio (“C6/C2”) from0.0001 to 0.1 (e.g., 0.0050), a constant hydrogen to ethylene molarratio (“H2/C2”) from 0.0001 to 0.1 (e.g., 0.0020), and a constantethylene (“C2”) partial pressure from 1,000 to 2,000 kilopascals (kPa)(e.g., 1,500 kPa). Measure concentrations of all gases by an in-line gaschromatograph to ensure relatively constant composition in the recyclegas stream. Maintain a reacting bed of growing polymer particles in afluidized state by continuously flowing a make-up feed and recycle gasthrough the reaction zone. Use a superficial gas velocity of from 0.4 to0.7 meter per second (m/sec) (e.g., from 0.49 to 0.67 m/sec, or 1.6 to2.2 feet per second (ft/sec)). Operate the Reactor at a total pressureof 2,000 to 3,000 kPa (e.g., 2344 to about 2413 kPa, or 340 to about 350pounds per square inch-gauge (psig)) and at a constant reactiontemperature of 85° to 115° C. (e.g., 105° C.). Maintain the fluidizedbed at a constant height by withdrawing a portion of the bed at a rateequal to the rate of formation of particulate product. The polymerproduction rate is in the range of 5 to 20 kg/hour (e.g., 13 to 18kg/hour. Remove the polymer product semi-continuously via a series ofvalves into a fixed volume chamber, wherein this removed polymer productis purged to remove entrained hydrocarbons and treated with a stream ofhumidified nitrogen (N2) gas to deactivate any trace quantities ofresidual polymerization catalyst. A polyethylene is made andcharacterized by melt index 12 (190 C., 2.16 kg, ASTM D1238-13); density(ASTM D792-13, Method B); Butyl branching frequency* (BBF, NMR), whereinBBF is the number of butyl branches per 1000 main chain carbon atoms;number average molecular weight; weight average molecular weight;molecular mass dispersity (M_(w)/M_(n)), Ð_(M) (pronounced D-stroke M),and melting temperature T_(m).

Inventive Example 10: synthesis of compound (8-2): compound (8) whereinR1 to R3 and R6 to R9 are H and R10, R4, and R5 are methyl. In a dryboxin a 120 milliliter (mL; 4-ounces) glass jar, slurried the(MeCp)ZrCl₃-DME complex (0.88 g, 2.85 mmol) in 20 mL of toluene. Stirredthe resulting mixture, and to it added compound (6-1) (0.5 g, 3.57 mmol)in small portions. Stirred the resulting reaction mixture for 48 hoursat room temperature, filtered, and removed the solvent under vacuum fromthe filtrate to give a brown solid crude product. Triturated the crudeproduct by slurrying it in 35 mL of pentane and stirring for 4 hours atroom temperature. Filtered the triturated mixture to give 0.28 gpurified solid compound (8-2) in 26% yield. ¹H NMR (400 MHz, Benzene-d₆)δ 5.86 (t, J=2.7 Hz, 2H), 5.76 (t, J=2.7 Hz, 2H), 5.35 (s, 1H),3.04-2.89 (m, 2H), 2.37-2.23 (m, 3H), 2.19 (s, 3H), 2.04-1.92 (m, 1H),1.67 (s, 6H).

Inventive Example 11: synthesis of compound (8-3): compound (8) whereinR1 to R3 and R6 to R9 are H, R10 is propyl, and R4 and R5 are methyl. Indrybox in a 120 mL glass jar, slurried the (PrCp)ZrCl₃-DME complex (1.13g, 2.85 mmol) in 20 mL of toluene. Stirred the resulting mixture, and toit added compound (6-1) (0.5 g, 3.57 mmol) in small portions. Stirredthe resulting reaction mixture for 48 hours at room temperature,filtered, and removed the solvent under vacuum from the filtrate to givea brown solid crude product. Triturated the crude product by slurryingit in pentane (20 mL), with stirring for 4 hours at room temperature.Filtered the triturated mixture, and triturated it with fresh pentane(20 mL) with stirring for 4 hours at room temperature. Filtered thesecond triturated mixture to give 0.28 g of purified solid compound(8-3) in 24% yield. ¹H NMR (400 MHz, Benzene-d₆) δ 5.97-5.85 (m, 2H),5.81-5.68 (m, 2H), 5.39 (s, 1H), 3.06-2.92 (m, 2H), 2.72-2.64 (m, 2H),2.38-2.22 (m, 3H), 2.06-1.93 (m, 1H), 1.69 (s, 6H), 1.58-1.39 (m, 3H),0.83 (t, J=7.4 Hz, 3H).

Inventive Example 12: synthesis of compound (8-4): compound (8) whereinR1 to R3 and R6 is H, and to R7 to R10 and R4 and R5 are methyl.Replicated Inventive Example 11 except used (Me₄Cp)ZrCl₃ (0.96 g, 2.85mmol) instead of the (PrCp)ZrCl₃-DME complex to give 0.57 g purifiedsolid compound (8-4) in 48% yield. ¹H NMR (400 MHz, Benzene-d₆) δ 5.41(s, 1H), 5.26 (s, 1H), 3.15-3.04 (m, 2H), 2.56-2.41 (m, 1H), 2.37 (dt,J=14.7, 8.5 Hz, 2H), 2.13-2.02 (m, 1H), 2.01 (s, 6H), 1.79 (s, 6H), 1.69(s, 6H).

Inventive Example 13: synthesis of compound (8a-1): compound (8a)wherein R4 and R5 are methyl. In a drybox in a 240 mL glass jar,slurried ZrCl₄-DME complex (0.83 g, 3.56 mmol) in 20 mL of toluene andstirred. Added 0.99 g (7.12 mmol) of compound (6-1) in small portions,and stirred the resulting reaction mixture for 48 hours at roomtemperature. Filtered and removed solvent from filtrate under vacuum togive brown solid. Triturated twice, each by slurrying in 40 mL ofpentane, stirring for 4 hours at room temperature, and filtering to give0.34 g purified solid compound (8-4) in 22% yield. ¹H NMR (400 MHz,Benzene-d₆) δ 5.40 (s, 2H), 3.09 (ddd, J=14.6, 8.6, 1.7 Hz, 4H),2.61-2.44 (m, 2H), 2.38 (dt, J=14.5, 8.5 Hz, 4H), 2.12-1.98 (m, 2H),1.75 (s, 12H).

Inventive Example 14: synthesis of compound (6-2): compound (6) whereinR1 to R3 is H, R4 is H and R5 is methyl via a sequence of reaction stepscomprising (14a) reduction, (14b) dehydration, and (14c) deprotonation.

Inventive Example 14a: synthesis of compound (4-2): compound (4) whereinR1 to R3 is H, and R4 is H and R5 is methyl. Under an atmosphere of drynitrogen, weighed the compound (3-1) of Inventive Example 2 (1.06 g,7.78 mmol) in a 250 mL round bottom flask, and dissolved it in anhydrousdiethyl ether (32 mL). In a separate 250 mL round bottom flask prepareda suspension of lithium aluminum hydride solution (1.0 M, 8.25 mL, 8.25mmol) in anhydrous diethyl ether (20 mL), and cooled the suspension to0° C. Added the solution in diethyl ether of compound (3-1) to thecooled lithium aluminum hydride suspension over 15 minutes, and stirredthe resulting reaction mixture at 0° C. for 1 hour. Decomposed excesslithium aluminum hydride by addition of water (20 mL). Separated theresulting organic phase from the aqueous layer and the inorganic salts.Extracted the aqueous layer with dichloromethane (3×50 mL). Combined theether and dichloromethane layers, and washed the combination with brine(50 mL), dried over magnesium sulfate and filtered. Removed solvent fromthe filtrate in vacuo to give 0.74 g of compound (4-2) in 69% yield.Compound (4-2) is characterized by GC/MS (EI) 138 (mass), 123, 95.

Inventive Example 14b: synthesis of compound (5-2): compound (5) whereinR1 to R3 is H, and R4 is H and R5 is methyl. Dissolved compound (4-2)(0.74 g, 5.35 mmol) in anhydrous diethyl ether (35 mL), and cooledsolution to 0° C. Added Amberlyst 15 acid resin (1.3 g) to the solution,and stirred the resulting reaction mixture for 1 hour at 0° C., andwarmed up to room temperature. Added magnesium sulfate and stirred themixture for 10 minutes. Filtered the mixture, and removed solvent fromthe filtrate in vacuo to give 0.49 g of compound (5-2) as a mixture ofisomers in 76% yield.

Inventive Example 14c: synthesis of compound (6-2): compound (6) whereinR1 to R3 is H, R4 is H, and R5 is methyl. In a glove box under anhydrousnitrogen atmosphere, dissolved compound (5-2) (0.49 g, 4.07 mmol) inpentane (20 mL) in a 250 mL round bottom flask. Cooled solution down to−35° C. for 20 minutes. To the stirred solution added dropwise asolution of n-butyl lithium in hexanes (1.6 M, 3.06 mL, 4.89 mmol).Stirred the resulting reaction mixture for 20 hours. Collected compound(6-2) by vacuum filtration, and washed the solid product with pentane,and dried under vacuum to give 0.12 g of compound (6-2) in 24% yield. ¹HNMR (400 MHz, THF-d₈) δ 5.35-5.16 (m, 1H), 2.26-2.01 (m, 2H), 1.98 (s,3H), 1.68-1.53 (m, 4H), 1.50-1.42 (m, 2H).

Inventive Examples 15 to 19: synthesis of spray-dried polymerizationcatalysts. In separate experiments, prepared a polymerization catalystsystem using one of polymerization catalysts of Inventive Example 6, 10,11, 12, and 13, respectively, as follows. Slurried 5.30 g of treated(hydrophobic) fumed silica (Cabosil TS-610) in 125 g of toluene. Thenadded 44 g of a 10 wt % solution of methylaluminoxane (MAO) in toluene.Next, added the polymerization catalyst of Inventive Example 6, 10, 11,12, or 13, and stirred the resulting mixture for 30 to 60 minutes. Useda spray-drier apparatus configured with an inlet and outlet and anatomizing device, a heated spray drier, and a cyclone separator.Introduced the resulting mixture into the spray-drier via the inlet intothe atomizing device, producing droplets that were then contacted with ahot nitrogen gas stream to evaporate the liquid and form a powder.Separated the powder from the gas mixture in the cyclone separator, anddischarged the separated fine powder through the outlet into an externalcontainer. During the foregoing spray-drying procedure, the spray driertemperature was set at 165° C. and the outlet temperature at 60° to 70°C. All loadings of the catalyst of Inventive Examples 6, 10, 11, 12, or13 were 50 micromoles of catalyst per gram of treated fumed silica(μmol/g), which corresponds to an Al:Zr atomic ratio of 100. This gave aspray-dried catalyst of Inventive Example 15, 16, 17, 18, or 19containing a polymerization catalyst of Inventive Example 6, 10, 11, 12,or 13, respectively.

Inventive Examples 20 to 24: lab-scale polymerization of ethylene and1-hexene using spray-dried catalyst of any one of Inventive Example 15,16, 17, 18, or 19 containing a polymerization catalyst of InventiveExample 6, 10, 11, 12, or 13, respectively. Used a 2-liter, stainlesssteel autoclave gas phase reactor equipped with a mechanical agitator.For each experimental run, first dried the reactor for 1 hour, thencharged the dried reactor with 400 g of NaCl and dried by heating at105° C. under nitrogen for 30 minutes. To the resulting dried reactor,added 5 g of SMAO (silica supported methylalumoxane) as a scavengerunder nitrogen pressure. Then sealed the reactor and stirred itscontents. Then charged the reactor with hydrogen (1500 ppm) and1-hexene. Pressurized the reactor with ethylene (total pressure=220 psi)to give H2/C2 molar ratio=0.0017 and C6/C2 molar ratio=0.004. Once thepressurized reactor reached a steady state, charged the spray-driedcatalyst of any one of Inventive Example 15, 16, 17, 18, or 19 thereintoto start a polymerization. Brought the reactor temperature to 100° C.,and maintained it at this temperature throughout the experiment run for60 minutes. At 60 minutes, cooled the reactor to room temperature ventedand opened. Washed the resulting product mixture with water, thenmethanol, and dried it to give a poly(ethylene-co-1-hexene) copolymer ofany one of Inventive Examples 20 to 24, respectively. Calculated thecatalyst activity in grams of polymer made per gram catalyst-hour asequal to a ratio of an amount of polymer yield to the amount of catalystadded to the reactor. Measured number-average molecular weight (Mn),weight average molecular weight (Mw), molecular weight distribution(Mw/Mn), melt temperature, and butyl branch frequency (BBF) according totheir foregoing respective test methods. Results are shown below inTable 1.

TABLE 1 Catalysts and copolymers of Inventive Examples 20 to 24.Catalyst Activity Melt Inv. Ex. (g copolymer/g temp. BBF (per No.Catalyst catalyst-hour) Mn Mw Mw/Mn (° C.) 1,000 C) 20 (8-1) 2,42914,237 46,784 3.29 132.70 0.69 (IE6) 21 (8-2) 3,311 17,998 45,438 2.52132.44 0.6 (IE10) 22 (8-3) 10,166 11,820 38,842 3.28 130.87 1.16 (IE11)23 (8-4) 1,528 9,586 22,922 2.39 133.21 N/d (IE12) 24 (8-a1) 2,28712,315 32,524 2.64 133.67 N/d (IE13) N/d means not detected at a limitof detection (LOD) of 0.1 to 0.2.

As shown in Table 1, the polymerizations of Inventive Examples 20 to 24using the polymerization catalysts (8-1), (8-2), (8-3), (8-4) and (8a-1)of Inventive Examples 6, 10, 11, 12, and 13, respectively, exhibitethylene and 1-hexene polymerization activity of at least 1500 gramspolymer/gram and produce a poly(ethylene-co-1-hexene) copolymer having adesirable degree of ethylene enchainment as evidence by the molecularweights of the resultant polymers. Each of the copolymers has a weightaverage molecular weight (Mw) of greater than 20,000, and the copolymersof Inventive Examples 20, 21, 22, 23, and 24 (corresponding to catalystsof Inventive Examples 6, 10, 11, 12 and 13) have butyl branch frequencyBBF of less than 1.5, preferably <1. Degree of ethylene enchainmentindicates the catalysts selectively permit polymerization of ethylene(i.e., improved ethylene enchainment) while mitigating thepolymerization of other molecules such as 1-hexene (e.g., via aparticular degree of steric hindrance associated with the substituentgroups of the catalysts).

As discussed earlier, Conia et al., Rand and Dolinski, and others reportusing PPA or P₂O₅/PPA mixture to catalyze a reaction of cycloheptene,cyclohexene, or cyclopentene with an alpha,beta-unsaturated carboxylicacid such as acrylic acid or crotonic acid gives a reaction mixture thatcontains an ester by-product (e.g., cycloheptyl crotonate, cyclohexylcrotonate, or cyclopentyl crotonate, respectively). We found that usinga sulfonic acid reagent (P₂O₅/H₃CSO₃H reagent) to catalyze a reaction ofcycloheptene, cyclohexene, or cyclopentene with analpha,beta-unsaturated carboxylic acid such as acrylic acid or crotonicacid gives a reaction mixture that does not contain an ester by-product(e.g., the reaction does not yield cycloheptyl crotonate, cyclohexylcrotonate, or cyclopentyl crotonate, respectively). We base this findingon analysis of at least one of the reaction mixtures by GC/MS (EI),which fails to show any ester by-product. We also base this finding onseeing that the reaction of cycloheptene, cyclohexene, or cyclopentenewith an alpha,beta-unsaturated carboxylic acid such as acrylic acid orcrotonic acid in the presence of the P₂O₅/H₃CSO₃H reagent goes muchfaster than a reaction of cycloheptyl crotonate, cyclohexyl crotonate,or cyclopentyl crotonate, respectively, in the presence of theP₂O₅/H₃CSO₃H reagent.

Without wishing to be bound by theory, we believe that the P₂O₅/H₃CSO₃Hreagent reacts with the alpha,beta-unsaturated carboxylic acid (e.g.,crotonic acid) to give in situ a mixed anhydride of general formulaR4CH═CHC(═O)—O—SO₂—CH₃, which generates in situ an acylium ion (i.e.,acyl carbonium ion) of formula R4CH═CHC⁺(═O), which rapidly undergoes aFriedel-Crafts acylation of cycloalkene to give in situ a ketone offormula R ^(a) —C(═O)—R ^(c) , wherein R ^(a) is R4CH═CH— and R ^(c) iscycloalken-1-yl, which ketone undergoes cyclization reaction to give thecorresponding cyclopentenone. For example, when the cycloalkene iscyclohexene and the alpha,beta-unsaturated carboxylic acid is crotonicacid, we believe that the P₂O₅/H₃CSO₃H reagent reacts with the crotonicacid to give in situ a mixed anhydride of general formulaH₃CCH═CHC(═O)—O—SO₂—CH₃, which generates in situ an acylium ion (i.e.,acyl carbonium ion) of formula H₃CCH═CHC⁺(═O), which rapidly undergoes aFriedel-Crafts acylation of cycloalkene to give in situ a ketone offormula R ^(a) —C(═O)—R ^(c) , wherein R ^(a) is H₃CCH═CH— and R ^(c) iscyclohexen-1-yl, which ketone undergoes cyclization reaction to give thecyclopentenone that is 2,3,4,5,6,7-hexahydro-3-methyl-1H-inden-1-one(i.e., 7-methyl-bicyclo[4.3.0]-7-nonen-9-one). Therefore, using theP₂O₅/H₃CSO₃H reagent in reaction of a cycloalkene such as cycloheptene,cyclohexene, or cyclopentene with an alpha,beta-unsaturated carboxylicacid such as acrylic acid or crotonic acid does not inherently make theester by-product (e.g., cycloheptyl crotonate, cyclohexyl crotonate, orcyclopentyl crotonate, respectively) reported by Conia et al., Rand andDolinski, and others using PPA or P₂O₅/PPA mixture.

The invention claimed is:
 1. A compound of formula (8):

wherein X is Cl or CH₃; R₁, R₂, and R₃ are independently H or(C₁-C₄)alkyl, or R₁ and R₃ are bonded together to form a (C₁-C₄)alkyleneand R₂ is H or (C₁-C₄)alkyl; R₄ is H or (C₁-C₄)alkyl; R₅ is H or(C₁-C₄)alkyl; R₆ to R₈ independently are H or (C₁-C₄)alkyl; and R₉ andR₁₀ independently are H or (C₁-C₄)alkyl, or R₉ and R₁₀ are bondedtogether and are a (C₃-C₅)alkylene.
 2. The compound of claim 1 selectedfrom the group consisting of compounds (8a), (8-1), (8-2), (8-3), and(8-4): compound (8a):

wherein R₄, R₅, R₆ and R₈ are independently as H or (C₁ -C₄)alkyl;compound (8-1): the compound (8) wherein X is Cl; R₁ to R₃ and R₆ to R₁₀are H; and R₄ and R₅ are methyl; compound (8-2): the compound (8)wherein X is Cl; R₁ to R₃ and R₆ to R₉ are H; and R₄, R₅, and R₁₀, aremethyl; compound (8-3): the compound (8) wherein X is Cl; R₁ to R₃ andR₆ to R₉ are H; R₄ and R₅ are methyl; and R₁₀ is propyl; and compound(8-4): the compound (8) wherein X is Cl; R₁ to R₃ and R₆ is H; and R₄,R₅, and R₇ to R₁₀ are methyl.
 3. The compound of claim 2 selected fromthe compound (8a).
 4. The compound of claim 2 selected from the compound(8-1).
 5. The compound of claim 2 selected from the compound (8-2). 6.The compound of claim 2 selected from the compound (8-3).
 7. Thecompound of claim 2 selected from the compound (8-4).
 8. The compound ofclaim 1 wherein X is CH₃.
 9. The compound of claim 1 selected from thegroup consisting of compounds (9a), (9-1), (9-2), (9-3), and (9-4):compound (9a):

wherein R₄, R₅, R₆ and R₈ are independently as H or (C₁ -C₄)alkyl;compound (9-1): the compound (8) wherein X is CH₃; R₁ to R₃ and R₆ toR₁₀ are H; and R₄ and R₅ are methyl; compound (9-2): the compound (8)wherein X is CH₃; R₁ to R₃ and R₆ to R₉ are H; and R₄, R₅, and R₁₀, aremethyl; compound (9-3): the compound (8) wherein X is CH₃; R₁ to R₃ andR₆ to R₉ are H; R₄ and R₅ are methyl; and R₁₀ is propyl; and compound(9-4): the compound (8) wherein X is CH₃; R₁ to R₃ and R₆ is H; and R₄,R₅, and R₇ to R₁₀ are methyl.
 10. The compound of claim 9 selected fromthe compound (9a).
 11. The compound of claim 9 selected from thecompound (9-1).
 12. The compound of claim 9 selected from the compound(9-2).
 13. The compound of claim 9 selected from the compound (9-3). 14.The compound of claim 9 selected from the compound (9-4).